Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_assertion description "[In contrast, a second group with more severe HbH disease has a non-deletional alpha-thalassemia defect instead of alpha+-thalassemia (genotype alpha alpha T/--SEA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_assertion evidence source_evidence_literature NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_assertion SIO_000772 2762043 NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_assertion wasDerivedFrom befree-20140225 NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_assertion wasGeneratedBy ECO_0000203 NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP235586.RAH0zWRhxreE995OS6ePmQc-KWmc-IFPEdHMnf-_Ttda8130_provenance.